CONICET | Buscador de Institutos y Recursos Humanos

A single exposure to amphetamine induces neurochemical sensitization in striatal areas. The neuropeptide angiotensin II, through AT1 receptors (AT1-R) activation, is involved in these responses. However, amphetamine-induced alterations can be extended to extrastriatal areas involved in blood pressure control and their physiological outcomes. Our aim for the present study was to analyze the possible role for AT1-R in these events using a twoinjection protocol and to further characterize the efficacy of the proposed AT1-R antagonism protocol. Central effect of orally administered AT1-R blocker (3mg/kg p.o. × 5 days) was analyzed recording spontaneous activity of the locus coeruleus. In another group of animals, pretreated with AT1-R blocker or vehicle, sensitization was achieved by a single administration of amphetamine (5mg/kg i.p- day 6) followed by a 3 week period off drug. After receiving an amphetamine challenge (0.5mg/kg i.p), we evaluated: 1) the sensitized cFos expression in locus coeruleus (LC), nucleus of the solitary tract (NTS), caudal ventrolateral medulla (A1) and central amygdala (CeAmy); and 2) the blood pressor response. AT1-R blockade decreased LC neurons? spontaneous firing rate. Moreover, sensitized c-Fos immunoreactivity was found in LC and NTS; and both responses were blunted by the AT1-R blocker pretreatment. Meanwhile, no differences were found neither in CeAmy nor A1. Sensitized pressor response was observed as sustained changes in mean arterial pressure and was effectively prevented by AT1-R blockade. Our results support the important role for brain AT1-R in amphetamine-induced sensitization, this time in extra-striatal areas and over its physiological outcome.